| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs776781782 | snp | A/G | 1.65866e-05 | 0.00287976 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365057 | GGAGAGCTAGTGGAA[A/G]GCTGGCTGGGAGGAA | 64412 |
| rs776851115 | snp | A/T | 1.66355e-05 | 0.002884 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365161 | GTGGGGGACTACAGG[A/T]GTCCCCAGGACCAAA | 64412 |
| rs776879862 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370816 | GTAGTTAGCAGTCTT[C/G]CTGGCTTCTCACTCT | 64412 |
| rs776958257 | snp | A/G | 3.75467e-05 | 0.00433266 | intron-variant | GZF1 | GRCh38.p7 | 20:23365772 | GAGCCGTCCGGAGGG[A/G]TCCCTGCGCACTGGA | 64412 |
| rs777062919 | snp | A/G | 1.65553e-05 | 0.00287705 | missense, intron-variant, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23369682 | GGGGAGAGGCCATTC[A/G]TGTGCAATGCGTGCG | 64412 |
| rs777351429 | snp | G/T | 1.80994e-05 | 0.00300822 | intron-variant | GZF1 | GRCh38.p7 | 20:23368727 | TGTTTTTAATGCCTG[G/T]ATTGTTTATGACTTT | 64412 |
| rs777363362 | snp | A/G | 4.95045e-05 | 0.00497492 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364954 | GAGAGAGCCAGCAAT[A/G]GCATGTCTTCAGATT | 64412 |
| rs777419522 | snp | A/G | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23368914 | TCACTGTACCAGCAT[A/G]TTAAAGTCCACACAG | 64412 |
| rs777498440 | snp | G/T | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364881 | TGCCCCCAGGGCAAG[G/T]GTGGCCACCGATGGC | 64412 |
| rs777588270 | snp | C/T | | | upstream-variant-2KB | LINC01431, GZF1 | GRCh38.p7 | 20:23360076 | GGTTTCACCATGTTG[C/T]CCAGGCTGGTCTTGA | 64412 |
| rs777631869 | snp | C/T | 1.64855e-05 | 0.00287097 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370350 | TGTCCCAGGACACCC[C/T]CCTGGCCACCACCAT | 64412 |
| rs777633743 | snp | A/G | 1.67262e-05 | 0.00289185 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365484 | CCTGAAGAGCCACCA[A/G]CGCCACGTGCACAGC | 64412 |
| rs777679434 | snp | C/T | 1.65427e-05 | 0.00287595 | missense, intron-variant, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23369655 | CTCCAGCGCCACCGC[C/T]GCATCCACACAGGGG | 64412 |
| rs777758152 | snp | C/T | 1.64792e-05 | 0.00287042 | synonymous-codon, missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370258 | TTTCCACAACCTGGC[C/T]GCAGTCCAAGACACT | 64412 |
| rs777850882 | snp | G/T | 3.29522e-05 | 0.00405894 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364539 | GGCCCACAAGGCAGT[G/T]CTGGCTGCCACCAGC | 64412 |
| rs777961192 | snp | A/C | | | upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23361530 | GGTGCGGTCCCGGCT[A/C]CTGGCGCGCCGAGCC | 64412 |
| rs778103641 | snp | C/T | 1.6734e-05 | 0.00289253 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364431 | ATCCTCCCCATTTAA[C/T]CTACTGCATGAGATG | 64412 |
| rs778205664 | snp | A/G | 6.65281e-05 | 0.00576711 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365152 | GAGGGTGATGTGGGG[A/G]ACTACAGGTGTCCCC | 64412 |
| rs778250114 | in-del | -/TTGT | 3.6152e-05 | 0.00425143 | intron-variant | GZF1 | GRCh38.p7 | 20:23368729 | TTTTTAATGCCTGTA[-/TTGT]TTATGACTTTATTTC | 64412 |
| rs778280458 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23372860 | CAAACTCCAAAGGGA[-/T]TGTGCAGCCTTTCGT | 64412 |
| rs778302954 | in-del | -/GCAATG | 1.64999e-05 | 0.00287222 | cds-indel, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364949 | CAGGAGAGAGAGCCA[-/GCAATG]GCATGTCTTCAGATT | 64412 |
| rs778520043 | snp | C/T | | | intron-variant | GZF1 | GRCh38.p7 | 20:23366382 | TCAAACCTAGGTCAG[C/T]CTTGGGTTAGCAGCA | 64412 |
| rs778591664 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23362216 | AGCGGACAGCGGCTG[C/T]AGCGGGGGCGCCGGC | 64412 |
| rs778594653 | snp | A/G | 1.69954e-05 | 0.00291503 | intron-variant | GZF1 | GRCh38.p7 | 20:23367148 | CTAGATCTAGAAGGA[A/G]ATGCAATTGATTAAT | 64412 |
| rs778609966 | snp | G/T | | | intron-variant | GZF1 | GRCh38.p7 | 20:23367561 | ATTCAGAGTAAGGGC[G/T]CTGAATGACATGAAA | 64412 |
| rs778646176 | snp | G/T | 1.65356e-05 | 0.00287533 | missense, intron-variant | GZF1 | GRCh38.p7 | 20:23367009 | TACTTTCAGAATTCA[G/T]ACAGGGGAAAAACCT | 64412 |
| rs778773081 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-3-prime, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370140 | TTGTCATTGTAGATG[C/G]CTCGCCCAAGAACGA | 64412 |
| rs778931237 | snp | A/G | 1.69444e-05 | 0.00291066 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365577 | GCGGCACGTGCTGCA[A/G]GTGCATGAGGGCGGC | 64412 |
| rs779049549 | snp | C/T | | | intron-variant, upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23362865 | GGTCTCCTCGAGGGC[C/T]CTGTTGGCAGAGGTC | 64412 |
| rs779077309 | snp | A/G | | | downstream-variant-500B | GZF1 | GRCh38.p7 | 20:23373534 | ACTGCTGATCTGACA[A/G]GGTGCACAGCTCAGG | 64412 |
| rs779082542 | in-del | -/TGCATGAGA | 1.6643e-05 | 0.00288465 | cds-indel, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364436 | CCCCATTTAACCTAC[-/TGCATGAGA]TGCATGAGCTTCGCC | 64412 |
| rs779249726 | snp | A/G | 1.67189e-05 | 0.00289122 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365462 | AGACCTTCGCCAACC[A/G]CTGCAACCTGAAGAG | 64412 |
| rs779284539 | snp | A/C | 1.66333e-05 | 0.00288381 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365115 | ATATACGAGAAGACT[A/C]CGAGAGCAGCAGAAA | 64412 |
| rs779414798 | snp | A/C | 0.00314122 | 0.0395062 | missense, intron-variant, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23369650 | ACGCCCTCCAGCGCC[A/C]CCGCCGCATCCACAC | 64412 |
| rs779583901 | snp | A/G | 4.62513e-05 | 0.00480869 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365739 | GTCCGCGCTCAAGAC[A/G]CACATGAGGTACGCG | 64412 |
| rs779606137 | snp | C/G | | | upstream-variant-2KB, intron-variant | GZF1 | GRCh38.p7 | 20:23361840 | CCAGAAGCCCGGAAT[C/G]GACGCGAAAGTGACC | 64412 |
| rs779607681 | snp | C/T | | | intron-variant | GZF1 | GRCh38.p7 | 20:23369377 | AGGCACATGTCCTGG[C/T]CCCTTTTTGGTGTAG | 64412 |
| rs779791091 | snp | C/G | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364693 | GTACAGGTGGAAGAA[C/G]ATCGGGTGCAGCGAA | 64412 |
| rs779911996 | snp | A/C | 1.66849e-05 | 0.00288828 | intron-variant | GZF1 | GRCh38.p7 | 20:23366987 | CTAAGTTATCATCTG[A/C]ATGTTGTACTTTCAG | 64412 |
| rs780098479 | snp | G/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364581 | GGAAGTGTTCCTTAA[G/T]GAGAAGAGTGTGGAT | 64412 |
| rs780125722 | snp | C/T | | | intron-variant, upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23362998 | TCTTATAGATCCCTT[C/T]CTTAGGCTTTGTCAG | 64412 |
| rs780184993 | snp | A/G | | | upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23360545 | TCCCAACCCTCTTCA[A/G]AAAGGTAGTGGAGAA | 64412 |
| rs780215435 | snp | C/T | | | intron-variant, upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23363819 | AAATTCTGAGGAGTT[C/T]AGGATGTTGGGAATG | 64412 |
| rs780311691 | snp | C/T | 6.68617e-05 | 0.00578155 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365451 | CACCTGCGGCCAGAC[C/T]TTCGCCAACCGCTGC | 64412 |
| rs780365039 | snp | A/G | 1.67075e-05 | 0.00289023 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365353 | TGCAGCATTTGCGAG[A/G]AGGCGTTTCTGTATG | 64412 |
| rs780388600 | snp | A/G | 1.65053e-05 | 0.0028727 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370115 | AAGAATACTCCATGG[A/G]AGTCTTTCCTTGTCA | 64412 |
| rs780416217 | in-del | -/TT | 3.30784e-05 | 0.0040667 | frameshift-variant, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370423 | CACACAGCTTCACTC[-/TT]TGAGCAACATGGAAT | 64412 |
| rs780418763 | snp | C/T | | | upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23360246 | CTGACCTCAAGTGAT[C/T]GGCCCGCCTCGGCCT | 64412 |
| rs780429188 | snp | G/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370595 | TAACTTGCACGGCTT[G/T]ATCACAGCATTTTTA | 64412 |
| rs780469196 | in-del | -/T | 0.000352559 | 0.0132723 | intron-variant | GZF1 | GRCh38.p7 | 20:23368959 | TCCCAGGGAAGGGAG[-/T]TTAGTTTGGCCAAAA | 64412 |
| rs780475993 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23372012 | TACTTCAAATTTAGT[G/T]ATGACAGTGTCACTG | 64412 |
| rs780481232 | snp | C/T | 1.71852e-05 | 0.00293127 | intron-variant | GZF1 | GRCh38.p7 | 20:23368753 | ACTTTATTTCATTTT[C/T]TCATGTAGGTGAAAG | 64412 |
| rs780582195 | snp | A/G | | | intron-variant | GZF1 | GRCh38.p7 | 20:23368166 | AAGGATTAAGTTAGA[A/G]TTGGTCCTTTGATAA | 64412 |
| rs780721876 | snp | A/C/T | 3.29838e-05 | 0.00406092 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370386 | AGCTTAGCGAGCTGA[A/C/T]CCCACAGACAGACTC | 64412 |
| rs780756101 | snp | A/G | 1.65094e-05 | 0.00287305 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364977 | TTCAGATTTGCCACC[A/G]AAGAAGTCCAAGGAC | 64412 |
| rs780831867 | snp | A/C/G | 0.000216211 | 0.0103954 | synonymous-codon, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365106 | TAAAAAGAAATATAC[A/C/G]AGAAGACTCCGAGAG | 64412 |
| rs780925612 | snp | A/G | 2.18835e-05 | 0.00330776 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365728 | TTCTCGCAGCCGTCC[A/G]CGCTCAAGACGCACA | 64412 |
| rs780987756 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23364559 | CTGCCACCAGCAAGT[C/T]TTTTAAGGAAGTGTT | 64412 |
| rs781064621 | in-del | -/TT | | | intron-variant | GZF1 | GRCh38.p7 | 20:23368740 | TGTATTGTTTATGAC[-/TT]TATTTCATTTTCTCA | 64412 |
| rs781319653 | snp | C/T | | | intron-variant, upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23363894 | AAAGTAGTTATTTAG[C/T]TGGTTCTTTTCAAAG | 64412 |
| rs781496222 | snp | A/C | | | downstream-variant-500B | GZF1 | GRCh38.p7 | 20:23373191 | ACAGCAGTCCCCAAC[A/C]TTTTTGGCACCAGGG | 64412 |
| rs781507739 | snp | C/T | 1.76129e-05 | 0.00296752 | intron-variant | GZF1 | GRCh38.p7 | 20:23369775 | TATTTGAGAAACAAG[C/T]TGCTGCCCTTAGATG | 64412 |
| rs781518295 | snp | C/T | | | intron-variant | GZF1 | GRCh38.p7 | 20:23368405 | TCTGATAAAGATCCA[C/T]AGAAGTGTTCCTTTG | 64412 |
| rs781593849 | snp | A/T | 1.65042e-05 | 0.0028726 | missense, intron-variant | GZF1 | GRCh38.p7 | 20:23367026 | CAGGGGAAAAACCTT[A/T]TGTCTGTGATGAATG | 64412 |
| rs781599041 | snp | A/G | | | upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23361044 | TCAAAGAGAGGAAAA[A/G]GTACTTACACTAATT | 64412 |
| rs781733847 | in-del | -/TA | 4.94254e-05 | 0.00497094 | frameshift-variant, utr-variant-3-prime, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23370190 | CAGCCTGACGAAGAG[-/TA]TGTGTCATCCAAGCT | 64412 |
| rs781777194 | snp | A/G | 3.3548e-05 | 0.00409547 | missense, nc-transcript-variant | GZF1 | GRCh38.p7 | 20:23365330 | AGAAGAAGAAGAGCA[A/G]CTTTAAGTGCAGCAT | 64412 |
| rs796445682 | snp | A/C | | | intron-variant, upstream-variant-2KB | GZF1 | GRCh38.p7 | 20:23363761 | AGCACAGCTTGTAAA[A/C]GCTGTGGAACTTAAC | 64412 |